Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

BACKGROUND: Several large, rare chromosomal copy number variants (CNVs) have recently been shown to increase risk for schizophrenia and other neuropsychiatric disorders including autism, ADHD, learning difficulties and epilepsy. AIMS: We wanted to examine the frequencies of these schizophrenia-assoc...

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Hlavní autoři: Grozeva, Detelina, Conrad, Donald F., Barnes, Chris P., Hurles, Matthew, Owen, Michael J., O'Donovan, Michael C., Craddock, Nick, Kirov, George
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2012
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3315675/
https://ncbi.nlm.nih.gov/pubmed/22130109
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.schres.2011.11.004
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